BIOTIS EMB AGAR HOLT-HARRIS

BIOTIS EMB AGAR HOLT-HARRIS is an FDA 510(k)-cleared medical device (K843763) manufactured by Otisville Biotech, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 9, 1984. Regulation: 8.